FDA UDI Not in Commercial Distribution 🇺🇸 United States

Rhino SRD

DI: 00865014000305 · Model: 1 · ENDO RX LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Rhino SRD
Primary DI
00865014000305
Version / Model
1
Catalog Number
Model 1
Company Name
ENDO RX LLC
Labeler DUNS
040304513
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-27
Public Version
4
Public Version Date
2020-11-19
Public Version Status
Update
Public Device Record Key
5595464a-6bde-4c74-af58-d50bfbc53fcd
Distribution End Date
2017-05-20

Device Description

Biliary Stone Removal Device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FGE Catheter, Biliary, Diagnostic
LQR Dislodger, Stone, Biliary

GMDN Terms

Code Name
46715 ERCP catheter, balloon, non-electrical, stone-retrieval

Identifiers

Type ID
Primary 00865014000305